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WO2007037824A2 - Procede de production en continu de resine silylee - Google Patents

Procede de production en continu de resine silylee Download PDF

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Publication number
WO2007037824A2
WO2007037824A2 PCT/US2006/032104 US2006032104W WO2007037824A2 WO 2007037824 A2 WO2007037824 A2 WO 2007037824A2 US 2006032104 W US2006032104 W US 2006032104W WO 2007037824 A2 WO2007037824 A2 WO 2007037824A2
Authority
WO
WIPO (PCT)
Prior art keywords
reaction zone
polyol
diisocyanate
continuously
silylating agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2006/032104
Other languages
English (en)
Other versions
WO2007037824A3 (fr
Inventor
John P. Banevicius
Misty Huang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
General Electric Co
Momentive Performance Materials Inc
Original Assignee
General Electric Co
Momentive Performance Materials Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to JP2008531115A priority Critical patent/JP5075126B2/ja
Priority to CA2622118A priority patent/CA2622118C/fr
Priority to KR1020087006197A priority patent/KR101329534B1/ko
Priority to AU2006295280A priority patent/AU2006295280A1/en
Priority to EP06801710.2A priority patent/EP1940915B1/fr
Priority to CN2006800338670A priority patent/CN101263178B/zh
Application filed by General Electric Co, Momentive Performance Materials Inc filed Critical General Electric Co
Priority to BRPI0615844A priority patent/BRPI0615844B1/pt
Publication of WO2007037824A2 publication Critical patent/WO2007037824A2/fr
Publication of WO2007037824A3 publication Critical patent/WO2007037824A3/fr
Priority to NO20081332A priority patent/NO20081332L/no
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00—Materials not provided for elsewhere
    • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
    • C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
    • C09K3/1021—Polyurethanes or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24—Stationary reactors without moving elements inside
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/0895—Manufacture of polymers by continuous processes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/71—Monoisocyanates or monoisothiocyanates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/71—Monoisocyanates or monoisothiocyanates
    • C08G18/718—Monoisocyanates or monoisothiocyanates containing silicon
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/329—Polymers modified by chemical after-treatment with organic compounds
    • C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2190/00—Compositions for sealing or packing joints

Definitions

  • This invention relates to a continuous ' process for preparing silane modified polyurethane resin and then, if required, feeding directly into a continuous compounding process to make a sealant/adhesive/coating in one production line.
  • the conventional method of making alkoxysilane modified polyurethane prepolymers is to react polyols with isocyanate materials batchwise at elevated temperatures.
  • the drawback of this well known method is long kettle time. Another drawback is difficult control of unwanted side reactions that increase viscosity. Another drawback is difficult scaleup from small units to larger production units.
  • the process comprises: (a) continuously introducing a predetermined quantity of a polyol into at least one reaction zone; (b) continuously introducing a silylating agent into the at least one reaction zone; (c) continuously reacting the polyol under reaction conditions of temperature and time sufficient to produce a silylated prepolymer resin; and, (d) continuously removing the silylated prepolymer resin from the at least one reaction zone.
  • FIG. 1 is a diagrammatic illustration of an embodiment of the process of the invention.
  • FIG. 2 is a diagrammatic illustration of another embodiment of the process of the invention.
  • the process and unit described here are useful for preparation of the prepolymers made of polyols, chain-extended or not, with silane modifiers.
  • the polyols have average molecular weight (Mn) of above about 1000.
  • the silane modifiers selected here contain functional groups which can react with either isocyanate or hydroxy groups.
  • Chain extender used can be aliphatic or aromatic diisocyanates. Catalysts are optional. All composition percentages or parts are by weight unless indicated otherwise.
  • the produced prepolymers can be continuously fed into next unit to make sealants, adhesives or coatings.
  • the unit described in this invention is a continuous process consisting of metering pumps and piping that deliver the ingredients to a continuous reactor where the ingredients are mixed, heated, provided time & mixing to allow reactions, then cooled and discharged to product storage, or fed to another unit to make a compounded product such as sealants, adhesives, or coatings.
  • multiple feed streams are employed to deliver the reactants to the one or more reactor tubes arranged in series at selected stages of the process.
  • the polyol is reacted with a polyisocyanate, the polyurethane product of this reaction being thereafter endcapped with a silylating agent such as an aminosilane or an isocyanatosilane.
  • a silylating agent such as an aminosilane or an isocyanatosilane.
  • an excess of polyol is employed so that the polyurethane is terminated with hydroxyl groups.
  • the endcapping silylating agent is an isocyanatosilane.
  • an excess of polyisocyanate is employed such that the resulting polyurethane is terminated with isocyanate groups.
  • the amonosilane is preferred.
  • the silylating agent is added to the reaction zone in a separate stream downstream of the entry point of the polyol and polyisocyanate to allow an appropriate amount of time for the polymerization reaction by to proceed before endapping.
  • polyisocyanate is optional.
  • the polyol is reacted with an isocyanatosilane to produce a resin product containing two urethane groups, i.e., the polyol itself is endcapped with silylated urethane groups.
  • polyisocyanates used in making the prepolymer may be an aliphatic, cycloaliphatic, araliphatic or aromatic polyisocyanate.
  • suitable polyisocyanates include ethylene diisocyanate, 1,6-hexamethylene diisocyanate, isophorone diisocyanate, cyclohexane-1,4- diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, p-xylylene diisocyanate, 1.4- phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'- diphenylmethane diisocyanate, 2,4'-diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanates and 1,5-naphthylene diisocyanate.
  • polyisocyanates can be used and also polyisocyanates which have been modified by the introduction of urethane, allophanate, urea, biuret, carbodiimide, uretonimine or isocyanurate residues.
  • Preferred isocyanates include toluene diisocyanate, diphenylmethane diisocyanate, polymeric diphenylmethane diisocyanate, cyclohexane diisocyanate, isophorone diisocyanate, naphthalene diisocyanate and phenylene diisocyanate.
  • the polymeric polyols may be members of any of the chemical classes of polymeric polyols used or proposed to be used in polyurethane formulations.
  • they may be polyesters, polyesteramides, polyethers, polythioethers, polycarbonates, polyacetals, polyolefins or polysiloxanes.
  • the polyols may contain free tertiary amino groups. Preferred molecular weights are above about 1000.
  • Polyester polyols which may be used include hydroxyl-terminated reaction products of polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, neopentyl glycol, 1,4-butanediol, furan dimethanol, cyclohexane dimethanol, glycerol, trimethylolpropane or pentaerythritol or mixtures thereof with polycarboxylic acids, especially dicarboxylic acids or their ester-forming derivatives, for example succinic, glutaric and adipic acids or their dimethyl esters, phthalic anhydride or dimethyl terephthalate.
  • polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, neopentyl glycol, 1,4-butanediol, furan dimethanol, cyclohexane dimethanol, glycerol, trimethylolpropane or pentaerythritol or mixtures thereof
  • Polyesters obtained by the polymerisation of lactones, for example caprolactone, in conjunction with a polyol may also be used.
  • Polyesteramides may be obtained by the inclusion of amino-alcohols such as ethanolamine in polyestei ⁇ fication mixtures.
  • Polyesters containing free tertiary amino groups may be obtained by including tertiary amino polyols, for example triethanolamine or N-metliyldiethanolamine in the polyesterification reaction.
  • Polyether polyols which may be used include products obtained by the polymerisation of a cyclic oxide, for example ethylene oxide, propylene oxide or tetrahydrofuran or by the addition of one or more such oxides to polyfunctional initiators, for example water, ethylene glycol, propylene glycol, diethylene glycol, cyclohexane dimethanol, glycerol, trimethylolpropane, pentaerythritol or Bisphenol A.
  • a cyclic oxide for example ethylene oxide, propylene oxide or tetrahydrofuran
  • polyfunctional initiators for example water, ethylene glycol, propylene glycol, diethylene glycol, cyclohexane dimethanol, glycerol, trimethylolpropane, pentaerythritol or Bisphenol A.
  • Especially useful polyethers include polyoxypropylene diols and triols, poly(oxyethylene- oxypropylene) diols and triols obtained by the simultaneous or sequential addition of ethylene and propylene oxides to appropriate initiators and polytetramethylene ether glycols obtained by the polymerisation of tetrahydrofuran.
  • Polyethers containing free tertiary amino groups may be obtained by the oxyalkylation, for example oxypropylation, of ammonia, primary or secondary amines and aminoalcohols.
  • suitable amines include ethylene diamine, aniline, benzylamine, toluene diamines, diaminodiphenylmethane and polymethylene polyphenyl polyamines.
  • Suitable aminoalcohols include ethanolamine, diethanolamine, triethanolamine, N- methyldiethanolamine, bis(2-hydroxyethyl)aniline, bis(2-hydroxypropyl)aniline and bis(2-hydroxyethyl)benzylamine.
  • mixtures of amino- containing and amino-free initiators may be used if desired.
  • Polythioether polyols which may be used include products obtained by condensing thiodiglycol either alone or with other glycols, dicarboxylic acids, formaldehyde, aminoalcohols or aminocarboxylic acids.
  • Polycarbonate polyols which may be used include products obtained by reacting diols such as 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, diethylene glycol or tetraethylene glycol with diaryl carbonates, for example diphenyl carbonate, or with phosgene.
  • diols such as 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, diethylene glycol or tetraethylene glycol
  • diaryl carbonates for example diphenyl carbonate, or with phosgene.
  • Polyacetal polyols which may be used include those prepared by reacting glycols such as diethylene glycol, Methylene glycol and hexanediol with formaldehyde. Suitable polyacetals may also be prepared by polymerising cyclic acetals.
  • Suitable polyolefin polyols include hydroxy-terminated butadiene homo- and copolymers.
  • Diols having pendent polyoxyethylene chains which may be used in the preparation of the prepolymer include those described in the prior art, for example in U.S. Pat. No. 3,905,929.
  • Silanes useful in the invention include isocyanatosilanes and aminosilanes.
  • the isocyanatosilane can be a selected from the group consisting of 3- isocyanatopropylmethyldimethoxysilane, 3-isocyanatopropyltrimetlioxysilane and 3- isocyanatopropyltriethoxysilane.
  • a suitable isocyanatosilane is available from GE Silicones under the designation A Link-35.
  • the aminosilanes can be, for example, selected from the group consisting of 4-amino-3,3-dimethylbutyltrimethoxysilane, 4- amino-3,3-dimethylbutyldimethoxymethylsilane, N-methyl-4-amino-3,3- dimethylbutyltrimethoxysilane, aminoisopropoxyethyltrimethoxysilane, aminoisopropoxypropyltrimethoxysilane, 4-amino-3,3-dimethylbutyltriethoxysilane, 4-amino-3,3-dimethylbutyldiethoxymethylsilane, N-methyl-4-amino-3,3- dimethylbutyltriethoxysilane and aminoisopropoxyethyltriethoxysilane.
  • Y is -NCO, -NHR, -NH 2 , or -HS,
  • R is an alkyl group having from 1-10 carbon atoms
  • R 1 is a divalent hydrocarbon group having from 1-10 carbon atoms, Me is methyl,
  • OR 2 is an alkoxy group wherein R 2 has from 1 to 5 carbon atoms (e.g., methoxy, ethoxy, propoxy, etc.), and
  • n 0 to 3.
  • the feeds can optionally include catalysts, plasticizers, colorants, stabilizers, thixotropes, fillers and the like.
  • Exemplary plasticizers include phthalates, dipropylene and diethylene glycol dibenzoates and mixtures thereof, epoxidized soybean oil and the like.
  • Useful sources of dioctyl and diisodecyl phthalate include those available under the tradenames "Jayflex DOP” and “Jayflex DIDP” from Exxon Chemical.
  • the dibenzoates are available as "Benzoflex 9-88", “Benzoflex 50” and “Benzoflex 400” from Velsicol Chemical Corporation.
  • the plasticizer typically comprises up to 100 parts per hundred parts of the polymer with 40 to 80 parts per hundred being preferred.
  • Typical fillers include reinforcing fillers such as fumed silica, precipitated silica and calcium carbonates.
  • reinforcing carbon black can be used as a main filler, leading to black systems.
  • Several commercial grades of carbon black useful in this invention are available, such as "Corax" products (Degussa). To obtain translucent formulations, higher levels of fumed silica or precipitated silica should be used as the main filler, without carbon black.
  • Treated calcium carbonates having particle sizes from 0.07 microns to 4 microns are preferred fillers and are available under several trade names, such as: “Ultra Pflex” and “Hi Pflex” from Specialty Minerals; “Winnofil SPM” and “Winnofil SPT” from Zeneca Resins; “Hubercarb IQt”, “Hubercarb 3Qt” and “Hubercarb W” from Huber and “Kotomite” from ECC. These fillers can be used either alone or in combination.
  • the fillers generally comprise up to 300 parts per 100 parts of the silylated polymer with 80 to 150 parts being the more preferred loading level.
  • UV stabilizers and/or antioxidants can be incorporated into the sealant formulations of this invention in an amount from 0 to 5 parts per hundred parts of silylated polymer with 0,5 to 2 parts being preferred.
  • These materials are available from companies such as Great Lakes and Ciba Specialty Chemicals under the tradenames "Anox 20” and “Uvasil 299 HM/LM” (Great Lakes), and "Irganox 1010,” “Irganox 1076,*” "Tinuvin 770,” “Tinuvin 327,” “Tinuvin 213” and “Tinuvin 622 LD” (Ciba), respectively.
  • the feed can include various thixotropic or anti-sagging agents.
  • This class of additives are typified by various castor waxes, fumed silica, treated clays and polyamides. These additives typically comprise 1 to 10 parts per hundred parts of silylated polymer component with 1 to 6 parts being preferred.
  • Useful thixotropes include those available as: “Aerosil” from Degussa, "Cab-O-Sil” from Cabot, “Castorwax” from CasChem, “Thixatrol” and “Thixcin” from Rheox, and "Disparlon” from King Industries.
  • Suitable catalysts are dialkyltin dicarboxylates, such as dibutyltin dilaurate and dibutyltin acetate, tertiary amines, the stannous salts of carboxylic acids, such as stannous octoate and stannous acetate, and the like.
  • the process includes metering of the reactants, mixing of the reactants (e.g., by static mixing elements in the tubular reactor(s), heating, drying, devolatilization, and grinding.
  • the products include silane terminated polyurethanes (SPUR) which, in one embodiment of the invention, can be thereafter incorporated into sealant/adhesive.
  • SPUR silane terminated polyurethanes
  • the sealant/adhesive can be produced by the continous process described herein by the addition into a feed stream of the appropriate additives as described above.
  • the reactor is a tubular reactor with an internal static mixer.
  • the ratio of length to diameter (LfD) can typically range from about 10:1 to about 50:1 although ratios outside of this range can be employed where appropriate, hi an embodiment of the invention the reaction is typically conducted at a temperature of up to about 200°C. hi another embodiment the reaction temperature can range from about 80 0 C to about 170 0 C. hi yet another embodiment the reaction temperature can range from about 120 0 C to about 150 0 C.
  • the reactants are linearly moved through the reactor(s).
  • the residence time of reactants in the tubular reactor can typically be up to about 30 minutes, although any suitable residence time can be selected.
  • the reactors are arranged in series and can be of different diameters and lengths.
  • the feed streams can be introduced at different points in the process.
  • Fl is a feed stream containing polyol, and optionally various sealant/adhesive/coating additives such as described above.
  • F2 is a feed stream containing a silylating agent (e.g., isocyanatosilane), which is introduced into the polyol feed stream Fl prior to entry into tubular reactor R.
  • F3 is a feed stream containing catalyst which is introduced into tubular reactor R downstream of the inlet into which combined feeds Fl and F2 are introduced.
  • Reactor R includes an internal static mixer and is heated by an external heat source to raise the contents of the reactor to the appropriate reaction temperature.
  • the length of reactor R and the throughput rate are adjusted to provide a desired residence time for the contents of the reactor as they are moved linearly therethrough.
  • An endapping reaction takes place in reactor R.
  • the effluent from reactor R is directed to a cooler C, which cools the effluent to about 20 degrees C.
  • the product is a silylated polyurethane SPUR.
  • a diisocyanate feed F5 is combined with polyol feed F4 prior to entry into reactor R-I.
  • a chain extension reaction occurs in reactor R-I.
  • the diisocyanate feed F5 also includes polyol.
  • the polyol feed F4 includes sealant/adhesive/coating additives such as described above.
  • a silylating agent feed F6 is introduced between reactors R-I and R-2. An endcapping reaction occurs in reactor R-2.
  • the silylating agent feed F6 can be introduced at other points in the process depending on the amount of chain extension desired.
  • Feed F7 includes a catalyst and is introduced between reactor R-2 and R-3. The effluent of reactor R-3 is sent to cooler C.
  • the product is a silylated polyurethane SPUR.
  • A-Link 35 (isocyanato silane from GE) was pumped continuously to the reactor, at a rate of approximately 3 cc/min, using a Milton Roy metering piston pump.
  • SUL-4 (dibutyltin dilaurate catalyst from Crompton) was preblended at 0.1% concentration with Acclaim 12,200; this preblend was pumped continuously to the reactor at approximately 5 cc/min, using a Zenith metering pump, size 0.584 cc/rev, operating at approximately 8.3 rpm.
  • the tubular reactor consisted of pipe containing internal static mixer elements (Koch- Sulzer SMX) to provide mixing.
  • the process set up was similar to that illustrated in FIG. 1.
  • the reactor was heated to approximately 100-180 degrees Celsius (C) using electrical heat tape on the pipe. Temperature was measured by thermocouples.
  • a cooling water jacketed section of pipe cooled the product to approximately 20-80 degrees C.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Sealing Material Composition (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

L'invention concerne un procédé de production en continu de prépolymère silylé consistant à introduire en continu une quantité prédéterminée d'un polyol dans au moins une zone de réaction; à introduire en continu un agent de silylation dans la zone de réaction; à faire réagir en continu le polyol dans des conditions de réaction de température et de temps suffisantes pour produire une résine de prépolymère silylée; et à éliminer en continu ladite résine de la zone de réaction.
PCT/US2006/032104 2005-09-14 2006-08-17 Procede de production en continu de resine silylee Ceased WO2007037824A2 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
CA2622118A CA2622118C (fr) 2005-09-14 2006-08-17 Procede de production en continu de resine silylee
KR1020087006197A KR101329534B1 (ko) 2005-09-14 2006-08-17 실릴화 레진의 연속 제조를 위한 방법
AU2006295280A AU2006295280A1 (en) 2005-09-14 2006-08-17 Process for the continuous production of silylated resin
EP06801710.2A EP1940915B1 (fr) 2005-09-14 2006-08-17 Procede de production en continu de resine silylee
CN2006800338670A CN101263178B (zh) 2005-09-14 2006-08-17 甲硅烷基化的树脂的连续生产方法
JP2008531115A JP5075126B2 (ja) 2005-09-14 2006-08-17 シリル化樹脂の連続的調製方法
BRPI0615844A BRPI0615844B1 (pt) 2005-09-14 2006-08-17 processo para a produção contínua de resina sililada
NO20081332A NO20081332L (no) 2005-09-14 2008-03-13 Fremgangsmate for kontinuerlig fremstilling av silylrelatert harpisk

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11/226,694 US7435787B2 (en) 2005-09-14 2005-09-14 Process for the continuous production of silylated resin
US11/226,694 2005-09-14

Publications (2)

Publication Number Publication Date
WO2007037824A2 true WO2007037824A2 (fr) 2007-04-05
WO2007037824A3 WO2007037824A3 (fr) 2007-05-31

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PCT/US2006/032104 Ceased WO2007037824A2 (fr) 2005-09-14 2006-08-17 Procede de production en continu de resine silylee

Country Status (12)

Country Link
US (1) US7435787B2 (fr)
EP (2) EP2287228B1 (fr)
JP (1) JP5075126B2 (fr)
KR (1) KR101329534B1 (fr)
CN (2) CN102898616B (fr)
AU (1) AU2006295280A1 (fr)
BR (1) BRPI0615844B1 (fr)
CA (1) CA2622118C (fr)
NO (1) NO20081332L (fr)
RU (1) RU2008114333A (fr)
TW (1) TWI397557B (fr)
WO (1) WO2007037824A2 (fr)

Cited By (6)

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US8637157B2 (en) 2011-02-28 2014-01-28 Momentive Performance Materials Inc. Copolycarbonates, their derivatives and the use thereof in silicone hardcoat compositions
WO2019008258A1 (fr) 2017-07-04 2019-01-10 Bostik Sa Preparation d'une composition adhesive dans une extrudeuse
EP3480234A1 (fr) 2017-11-03 2019-05-08 Evonik Degussa GmbH Copolymères séquencés contentant des motifs structuraux polyester et polyoléfine et ses utilisations
WO2019086533A1 (fr) 2017-11-03 2019-05-09 Evonik Degussa Gmbh Formulations contenant des copolymères à blocs et leur utilisation
EP4386025A1 (fr) 2022-12-15 2024-06-19 Aurotec GmbH Procédé et réacteur modulaire pour produire un prépolymère
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BRPI0615844B1 (pt) 2018-05-08
CN102898616B (zh) 2015-06-24
CN101263178B (zh) 2012-11-14
US20070060735A1 (en) 2007-03-15
NO20081332L (no) 2008-06-09
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RU2008114333A (ru) 2009-10-20
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CA2622118C (fr) 2015-03-24
EP2287228B1 (fr) 2013-05-08
BRPI0615844A2 (pt) 2011-05-31
EP1940915B1 (fr) 2013-04-17
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EP1940915A2 (fr) 2008-07-09
EP2287228A3 (fr) 2011-03-30
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CN102898616A (zh) 2013-01-30
CN101263178A (zh) 2008-09-10
JP5075126B2 (ja) 2012-11-14
CA2622118A1 (fr) 2007-04-05
EP2287228A2 (fr) 2011-02-23

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